Publications by authors named "Amanda R Dahl"

Objective: Type 1 diabetes autoantibodies are directed against multiple antigens including: glutamic acid decarboxylase, protein tyrosine phosphatase-like islet antigen 2 (IA2), insulin (IAA), and Zinc transporter 8 protein (ZnT8). The aim of our study was to determine if the presence or titer of ZnT8 antibodies (Ab) was predictive for clinical presentation at diagnosis or for the subsequent disease course.

Methods: Between January, 2003 and May, 2019, 105 patients aged ≤21 years with a clinical diagnosis of type 1 diabetes mellitus had at least 1 autoantibody measured.

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Congenital nephrotic syndrome (CNS) is a complex condition that requires multidisciplinary care. Hyperlipidemia is a characteristic feature with elevation of serum cholesterol and triglycerides. Little evidence is available to guide treatment of dyslipidemia in infants with CNS.

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Mutations in the hepatocyte nuclear factor-1-beta () gene cause a variety of diseases in different organ systems. Mutations have been described as causing neonatal cholestasis, maturity-onset diabetes of the young (type 5), cortical renal cysts, urogenital abnormalities, liver dysfunction, and atrophy of the pancreas. We describe a male patient who presented with cholestatic liver disease in infancy which progressed by age 14 to end-stage liver disease due to HNF1B disease.

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Background: There is a lack of consensus on the cardiometabolic consequences of mild subclinical hypothyroidism (SCH) among children. The objective of the current study was to compare lipid profiles in children with mild SCH with those of euthyroid children.

Study Design: Retrospective medical record review.

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Severe obesity is associated with abnormal lipids and increased risk for cardiovascular disease. Obesity is a risk factor for vitamin D deficiency. We examined relationship between 25-hydroxy vitamin D (25(OH)D) concentrations and lipids in children with severe obesity.

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Article Synopsis
  • Klinefelter syndrome, a common chromosomal condition in males, is associated with increased risks for type 1 and type 2 diabetes, with few reported cases of neonatal diabetes linked to it.
  • This study documents a rare case where a 78-day-old male infant with Klinefelter syndrome developed transient neonatal diabetes due to a genetic mutation in the KCNJ11 gene following surgery for a heart defect.
  • The infant initially required insulin treatment but was weaned off by seven months, and at 34 months, he shows normal glucose levels, highlighting the need for continued monitoring of his condition.
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